Trial | NCT03208179  Report issue

Title

Improving PRegnancy Outcomes With Intermittent preVEntive Treatment in Africa
IPTp With Dihydroartemisinin-piperaquine and Azithromycin for Malaria, Sexually Transmitted and Reproductive Tract Infections in Pregnancy in High Sulphadoxine-pyrimethamine Resistance Areas in Kenya, Malawi and Tanzania

  • Phase

    Phase 3

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    4680
This study evaluates the efficacy and safety of monthly intermittent preventive treatment using dihydroartemisinin piperaquine (DP) alone or in combination with azithromycin (AZ) compared to sulphadoxine-pyrimethamine (SP) for the prevention of malaria in pregnant women in the second and third trimester.
Intermittent preventive treatment with sulphadoxine-pyrimethamine (IPTp-SP) is one of the pillars of malaria prevention in pregnancy in sub-Saharan Africa, in addition to prompt case management and use of long lasting insecticide treated bednets. However, mounting resistance to SP by Plasmodium falciparum increasing renders IPTP-SP ineffective.

Two exploratory trials in Uganda and Kenya demonstrated that IPTp with DP was superior to IPTp-SP for the prevention of malaria infection in pregnancy. However, neither study was adequately powered to look at adverse birth outcomes. This study is a confirmatory efficacy trial in Malawi, Tanzania and Kenya to determine the efficacy and safety of IPTp with DP alone or in combination with AZ.

This will be a 3-arm trial, superiority, partial blinded, placebo controlled, randomized trial comparing IPTp with SP, versus IPTp with DP alone, and IPTp with DP+AZ with the following hypotheses:

IPTp with DP is superior to IPTp with SP in preventing adverse pregnancy outcomes.
The combination of DP with AZ further reduces adverse pregnancy outcomes compared to IPTp with DP alone.
Study Started
Mar 29
2018
Primary Completion
Mar 15
2020
Study Completion
Mar 15
2020
Last Update
Jun 27
2022

Drug dihydroartemisinin-piperaquine

Women randomised to this intervention will receive 3 day treatment dose of dihydroartemisinin-piperaquine by body weight plus azithromycin placebo

  • Other names: Eurartesim

Drug sulphadoxine-pyrimethamine

Women randomised to this intervention will receive stat dose of 3 tablets of 500 mg sulphadoxine and 25 mg of pyrimethamine each (total dose of 1,500mg sulphadoxine and 75mg pyrimethamine) on a single day of clinic visit

  • Other names: Fansidar

Drug dihydroartemisinin-piperaquine plus azithromycin

Women randomised to this intervention will receive 3 day treatment dose of dihydroartemisinin-piperaquine by body weight plus azithromycin (500mg)

  • Other names: Eurartesim plus Zithromax

IPTp-SP Active Comparator

Stat course of 3 tablets of quality-assured SP (tablets of 500 mg of sulphadoxine and 25 mg of pyrimethamine) at each scheduled antenatal visit

IPTp-DP Experimental

Dihydroartemisinin-piperaquine [3 to 5 tablets of DP (tablets of 40 mg of dihydroartemisinin and 320 mg of piperaquine, based on bodyweight) daily for 3 days] + placebo AZ at each scheduled antenatal visit

IPTp-DPAZ Experimental

Dihydroartemisinin-piperaquine [3 to 5 tablets of DP (tablets of 40 mg of dihydroartemisinin and 320 mg of piperaquine, based on bodyweight) daily for 3 days] + AZ tablet [1.5g over 3 days as 500mg per day] at each scheduled antenatal visit.

Criteria 

Inclusion Criteria:

Pregnant women between 16-28 weeks' gestation
Viable singleton pregnancy
Resident of the study area
Willing to adhere to scheduled and unscheduled study visit procedures
Willing to deliver in a study clinic or hospital
Provide written informed consent

Exclusion Criteria:

Multiple pregnancies (i.e. twin/triplets)
HIV-positive
Known heart ailment
Severe malformations or non-viable pregnancy if observed by ultrasound
History of receiving IPTp-SP during this current pregnancy
Unable to give consent
Known allergy or contraindication to any of the study drugs
No Results Posted